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Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug
Middle East Respiratory Syndrome (MERS) is a respiratory disease caused by a coronavirus (MERS-CoV). Since its emergence in 2012, nosocomial amplifications have led to its high epidemic potential and mortality rate of 34.5%. To date, there is an unmet need for vaccines and specific therapeutics for...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726485/ https://www.ncbi.nlm.nih.gov/pubmed/33309540 http://dx.doi.org/10.1016/j.antiviral.2020.104996 |
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author | Gan, Hanjie Jonathan Harikishore, Amaravadhi Lee, Jihye Jeon, Sangeun Rajan, Sreekanth Chen, Ming Wei Neo, Jun Long Kim, Seungtaek Yoon, Ho Sup |
author_facet | Gan, Hanjie Jonathan Harikishore, Amaravadhi Lee, Jihye Jeon, Sangeun Rajan, Sreekanth Chen, Ming Wei Neo, Jun Long Kim, Seungtaek Yoon, Ho Sup |
author_sort | Gan, Hanjie Jonathan |
collection | PubMed |
description | Middle East Respiratory Syndrome (MERS) is a respiratory disease caused by a coronavirus (MERS-CoV). Since its emergence in 2012, nosocomial amplifications have led to its high epidemic potential and mortality rate of 34.5%. To date, there is an unmet need for vaccines and specific therapeutics for this disease. Available treatments are either supportive medications in use for other diseases or those lacking specificity requiring higher doses. The viral infection mode is initiated by the attachment of the viral spike glycoprotein to the human Dipeptidyl Peptidase IV (DPP4). Our attempts to screen antivirals against MERS led us to identify montelukast sodium hydrate (MSH), an FDA-approved anti-asthma drug, as an agent attenuating MERS-CoV infection. We showed that MSH directly binds to MERS-CoV-Receptor-Binding Domain (RBD) and inhibits its molecular interaction with DPP4 in a dose-dependent manner. Our cell-based inhibition assays using MERS pseudovirions demonstrated that viral infection was significantly inhibited by MSH and was further validated using infectious MERS-CoV culture. Thus, we propose MSH as a potential candidate for therapeutic developments against MERS-CoV infections. |
format | Online Article Text |
id | pubmed-7726485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77264852020-12-10 Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug Gan, Hanjie Jonathan Harikishore, Amaravadhi Lee, Jihye Jeon, Sangeun Rajan, Sreekanth Chen, Ming Wei Neo, Jun Long Kim, Seungtaek Yoon, Ho Sup Antiviral Res Article Middle East Respiratory Syndrome (MERS) is a respiratory disease caused by a coronavirus (MERS-CoV). Since its emergence in 2012, nosocomial amplifications have led to its high epidemic potential and mortality rate of 34.5%. To date, there is an unmet need for vaccines and specific therapeutics for this disease. Available treatments are either supportive medications in use for other diseases or those lacking specificity requiring higher doses. The viral infection mode is initiated by the attachment of the viral spike glycoprotein to the human Dipeptidyl Peptidase IV (DPP4). Our attempts to screen antivirals against MERS led us to identify montelukast sodium hydrate (MSH), an FDA-approved anti-asthma drug, as an agent attenuating MERS-CoV infection. We showed that MSH directly binds to MERS-CoV-Receptor-Binding Domain (RBD) and inhibits its molecular interaction with DPP4 in a dose-dependent manner. Our cell-based inhibition assays using MERS pseudovirions demonstrated that viral infection was significantly inhibited by MSH and was further validated using infectious MERS-CoV culture. Thus, we propose MSH as a potential candidate for therapeutic developments against MERS-CoV infections. Elsevier B.V. 2021-01 2020-12-10 /pmc/articles/PMC7726485/ /pubmed/33309540 http://dx.doi.org/10.1016/j.antiviral.2020.104996 Text en © 2020 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Gan, Hanjie Jonathan Harikishore, Amaravadhi Lee, Jihye Jeon, Sangeun Rajan, Sreekanth Chen, Ming Wei Neo, Jun Long Kim, Seungtaek Yoon, Ho Sup Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug |
title | Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug |
title_full | Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug |
title_fullStr | Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug |
title_full_unstemmed | Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug |
title_short | Antiviral activity against Middle East Respiratory Syndrome coronavirus by Montelukast, an anti-asthma drug |
title_sort | antiviral activity against middle east respiratory syndrome coronavirus by montelukast, an anti-asthma drug |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726485/ https://www.ncbi.nlm.nih.gov/pubmed/33309540 http://dx.doi.org/10.1016/j.antiviral.2020.104996 |
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